Natalia Volfovsky

4.5k total citations
29 papers, 1.7k citations indexed

About

Natalia Volfovsky is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Natalia Volfovsky has authored 29 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Natalia Volfovsky's work include RNA and protein synthesis mechanisms (10 papers), Genomics and Phylogenetic Studies (9 papers) and Genomics and Chromatin Dynamics (9 papers). Natalia Volfovsky is often cited by papers focused on RNA and protein synthesis mechanisms (10 papers), Genomics and Phylogenetic Studies (9 papers) and Genomics and Chromatin Dynamics (9 papers). Natalia Volfovsky collaborates with scholars based in United States, Russia and Poland. Natalia Volfovsky's co-authors include Robert M. Stephens, Steven L. Salzberg, Brian J. Haas, Alex Lash, Ran Zhang, Aaron K. Wong, Alicja Tadych, Vicky Yao, Chandra L. Theesfeld and Ming Yi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Natalia Volfovsky

28 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Natalia Volfovsky United States 20 1.3k 413 351 321 150 29 1.7k
Jun Yin China 23 1.3k 1.0× 418 1.0× 412 1.2× 248 0.8× 146 1.0× 79 2.0k
Fabian Grubert United States 18 2.3k 1.8× 448 1.1× 821 2.3× 519 1.6× 58 0.4× 20 2.8k
Diane I. Schroeder United States 15 1.2k 1.0× 145 0.4× 538 1.5× 130 0.4× 118 0.8× 18 1.6k
Karin Schmitt United States 17 973 0.8× 164 0.4× 914 2.6× 204 0.6× 65 0.4× 30 1.8k
Bettina A. Moser United States 27 2.0k 1.6× 151 0.4× 636 1.8× 212 0.7× 93 0.6× 50 2.5k
Ana Claudia Marques Switzerland 22 1.9k 1.5× 1.2k 2.8× 474 1.4× 389 1.2× 46 0.3× 36 2.5k
Javier Santoyo‐López Spain 19 1.7k 1.3× 312 0.8× 363 1.0× 176 0.5× 38 0.3× 30 2.3k
Edward A. Sekinger United States 9 1.7k 1.3× 208 0.5× 548 1.6× 212 0.7× 246 1.6× 12 2.0k
Zhiyu Peng China 23 1.4k 1.1× 254 0.6× 753 2.1× 980 3.1× 33 0.2× 87 2.6k
Paul A. Ginno United States 10 2.5k 2.0× 259 0.6× 454 1.3× 269 0.8× 23 0.2× 12 2.8k

Countries citing papers authored by Natalia Volfovsky

Since Specialization
Citations

This map shows the geographic impact of Natalia Volfovsky's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Natalia Volfovsky with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natalia Volfovsky more than expected).

Fields of papers citing papers by Natalia Volfovsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalia Volfovsky. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Natalia Volfovsky. The network helps show where Natalia Volfovsky may publish in the future.

Co-authorship network of co-authors of Natalia Volfovsky

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia Volfovsky. A scholar is included among the top collaborators of Natalia Volfovsky based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Natalia Volfovsky. Natalia Volfovsky is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Cokol, Murat, Zohar Weinstein, Kevin Shi, et al.. (2025). Analyzing the large and complex SFARI autism cohort data using the Genotypes and Phenotypes in Families (GPF) platform. Genome Research. 35(10). 2352–2362.
2.
Buja, Andreas, Natalia Volfovsky, Abba Μ. Krieger, et al.. (2018). Damaging de novo mutations diminish motor skills in children on the autism spectrum. Proceedings of the National Academy of Sciences. 115(8). E1859–E1866. 44 indexed citations
3.
Krishnan, Arjun, Ran Zhang, Vicky Yao, et al.. (2016). Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder. Nature Neuroscience. 19(11). 1454–1462. 265 indexed citations
4.
Teplyuk, Nadiya M., Erik J. Uhlmann, Galina Gabriely, et al.. (2016). Therapeutic potential of targeting micro RNA ‐10b in established intracranial glioblastoma: first steps toward the clinic. EMBO Molecular Medicine. 8(3). 268–287. 110 indexed citations
5.
Baugh, Evan H., Christian L. Müller, Rebecca F. Alford, et al.. (2016). Robust classification of protein variation using structural modelling and large-scale data integration. Nucleic Acids Research. 44(6). 2501–2513. 41 indexed citations
6.
Yang, Hui, et al.. (2014). GAP-Seq: a method for identification of DNA palindromes. BMC Genomics. 15(1). 394–394. 9 indexed citations
7.
Shulzhenko, Natalia, Anatoly Yambartsev, Mark Rochman, et al.. (2013). Gene network reconstruction reveals cell cycle and antiviral genes as major drivers of cervical cancer. Nature Communications. 4(1). 1806–1806. 61 indexed citations
8.
Hudson, Robert, Ming Yi, Natalia Volfovsky, et al.. (2013). Transcription signatures encoded by ultraconserved genomic regions in human prostate cancer. Molecular Cancer. 12(1). 13–13. 51 indexed citations
9.
Bacolla, Albino, Nuri A. Temiz, Ming Yi, et al.. (2013). Guanine Holes Are Prominent Targets for Mutation in Cancer and Inherited Disease. PLoS Genetics. 9(9). e1003816–e1003816. 33 indexed citations
10.
Shao, Wei, Valerie F. Boltz, Jonathan Spindler, et al.. (2013). Analysis of 454 sequencing error rate, error sources, and artifact recombination for detection of Low-frequency drug resistance mutations in HIV-1 DNA. Retrovirology. 10(1). 18–18. 81 indexed citations
11.
Li, Jingfeng, Keiko Akagi, Yongjun Hu, et al.. (2012). Mouse endogenous retroviruses can trigger premature transcriptional termination at a distance. Genome Research. 22(5). 870–884. 38 indexed citations
12.
Cer, Regina Z., Duncan Donohue, Uma Mudunuri, et al.. (2012). Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools. Nucleic Acids Research. 41(D1). D94–D100. 129 indexed citations
13.
Marshall, Vickie, Elisa Martró, Nazzarena Labò, et al.. (2010). Kaposi Sarcoma (KS)–Associated Herpesvirus MicroRNA Sequence Analysis and KS Risk in a European AIDS‐KS Case Control Study. The Journal of Infectious Diseases. 202(7). 1126–1135. 25 indexed citations
14.
Cer, Regina Z., Uma Mudunuri, Ming Yi, et al.. (2010). Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes. Nucleic Acids Research. 39(Database). D383–D391. 76 indexed citations
15.
Hüppi, Konrad, Natalia Volfovsky, Tamara L. Jones, et al.. (2008). The Identification of MicroRNAs in a Genomically Unstable Region of Human Chromosome 8q24. Molecular Cancer Research. 6(2). 212–221. 150 indexed citations
16.
Akagi, Keiko, Jingfeng Li, Robert M. Stephens, Natalia Volfovsky, & David E. Symer. (2008). Extensive variation between inbred mouse strains due to endogenous L1 retrotransposition. Genome Research. 18(6). 869–880. 69 indexed citations
17.
Hüppi, Konrad, Natalia Volfovsky, Mark Mackiewicz, et al.. (2006). MicroRNAs and genomic instability. Seminars in Cancer Biology. 17(1). 65–73. 72 indexed citations
18.
Volfovsky, Natalia, Brian J. Haas, & Steven L. Salzberg. (2003). Computational Discovery of Internal Micro-Exons. Genome Research. 13(6a). 1216–1221. 58 indexed citations
19.
Haas, Brian J., Natalia Volfovsky, Christopher D. Town, et al.. (2002). Full-length messenger RNA sequences greatly improve genome annotation. Genome biology. 3(6). RESEARCH0029–RESEARCH0029. 146 indexed citations
20.
Volfovsky, Natalia, Brian J. Haas, & Steven L. Salzberg. (2001). A clustering method for repeat analysis in DNA sequences. Genome biology. 2(8). RESEARCH0027–RESEARCH0027. 105 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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